Executive Development Programme in IVD Regulatory Affairs Strategies
-- ViewingNowThe Executive Development Programme in IVD Regulatory Affairs Strategies certificate course is a comprehensive program designed to meet the growing industry demand for professionals with expertise in regulatory affairs for In Vitro Diagnostic (IVD) devices. This course emphasizes the importance of understanding and navigating the complex regulatory landscape to ensure compliance and drive business success.
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⢠IVD Regulatory Affairs Overview
⢠Global IVD Regulations and Guidelines
⢠IVD Classification and Product Coding
⢠Quality Management Systems in IVD Regulatory Affairs
⢠IVD Clinical Evidence and Evaluation
⢠IVD Regulatory Submissions and Approvals
⢠Post-Market Surveillance and Vigilance in IVD Regulatory Affairs
⢠IVD Labeling, Packaging, and Distribution
⢠International IVD Regulatory Strategies and Compliance
⢠Trends and Future Perspectives in IVD Regulatory Affairs
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